A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv855304



Internal ID16149260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28598169..28610911hg38UCSC Ensembl
Innerchr16:28609490..28622232hg19UCSC Ensembl
Innerchr16:28516991..28529733hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3812743
hg1912743
hg1812743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571752
Supporting Variants
Samples
Known GenesSULT1A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv855304
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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